A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18249147



Internal ID20816187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:6154136..6154574hg38UCSC Ensembl
chr19:6154147..6154585hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38439
hg19439
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6599180
Supporting Variants
Samples
Known GenesACSBG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18249147
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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